(Natural News) The spike protein outer shell of the coronavirus contains “prion-like regions” that give the virus very high adhesion to ACE2 receptors in the human body. This has been documented by a study entitled, “SARS-CoV-2 Prion-Like Domains in Spike Proteins Enable Higher Affinity to ACE2,” published by the Human Microbiology Institute:
The presence and unique distribution of prion-like domains in the SARS-CoV-2 receptor-binding domains of the spike protein is particularly interesting, since although the SARS-CoV-2 and SARS-CoV S proteins share the same host cell receptor, angiotensin-converting enzyme 2 (ACE2), SARS-CoV-2 demonstrates a 10- to 20-fold higher affinity for ACE2
The mRNA vaccine works by hijacking your body’s cells and causing them to churn out proteins modeled after the spike proteins in the SARS-cov-2 coronavirus. Since that structure includes prion-like regions, random errors in mRNA sequences — which may be truncated by the human immune system before they reach the ribosomes in the cells — could cause mRNA vaccine recipients to churn out prions in their own bodies.
The risk of this was assessed by Dr. J. Bart Classen, who authored a paper in Microbiology & Infectious Diseases: “Covid-19 RNA Based Vaccines and the Risk of Prion Disease.” You can see the text of the study at this link.
That study concludes, “The results indicate that the vaccine RNA has specific sequences that may induce TDP-43 and FUS to fold into their pathologic prion confirmations.”
It also explains:
The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases.
The Mayo Clinic says CJD, the disease caused by prions, is 100% fatal and has no treatment.
Some of the symptoms of CJD (prion disease) described by the Mayo Clinic include: